Taiwan FDA registration 9a61ff440d6e64d09073a12bb2b1dea1

"Heavy Dimension Omby" in vitro assembly lower limb prosthesis (unsterilized)

TW: “重維歐恩比”體外組裝下肢義肢 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·Heavy Maintenance Rehabilitation Products Co., Ltd·Registered Mar 03, 2008 – Mar 03, 2023Expired
Registration details
Analysis ID
9a61ff440d6e64d09073a12bb2b1dea1
Company information
Manufacturer Country
Taiwan, Province of China
Product details
Intended Use
Limited to the first level recognition range of the in vitro assembly of lower limb prosthetics (O.3500) in the management measures for medical devices.
Product Type (Level 1)
o Physical Medical Sciences
Product Type (Level 2)
O.3500 shades
Import Information
Domestic
Dates and status
Registration Date
Mar 03, 2008
Expiry Date
Mar 03, 2023
About this record

Access comprehensive regulatory information for "Heavy Dimension Omby" in vitro assembly lower limb prosthesis (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9a61ff440d6e64d09073a12bb2b1dea1 and manufactured by Heavy Maintenance Rehabilitation Products Co., Ltd. The authorized representative in Taiwan is Heavy Maintenance Rehabilitation Products Co., Ltd.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

Free DatabasePowered by Pure Global AI89,000+ Devices